FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MANI NEEDLE & SUTURE PACK (PGA ABSORBABLE)
K Number: K053636
·
Decision Mar 14, 2006
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
142
Applicant Total
4
Review Days
75
Basic Information
- Device Name
- MANI NEEDLE & SUTURE PACK (PGA ABSORBABLE)
- K Number
- K053636
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4493
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MANI, INC.
- Date Received
- December 29, 2005
- Decision Date
- March 14, 2006
- Product Code
- GAM
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid | FDA class 2 | General, Plastic Surgery |
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